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Tag Archives: Validation

Estimation of Rabeprazole Sodium in tablet dosage form by using UV-VIS Spectrophotometer

About author Vipin Kumar Agrawal *, Alok Singh , Pravesh Kumar, Jyoti Rai, Inamullah Department of Pharmaceutics, Invertis Institute of Pharmacy, Invertis University, Bareilly-243 123, Uttar Pradesh, India Department of Pharmaceutical Chemistry, Invertis Institute of Pharmacy, Invertis University, Bareilly-243 123, Uttar Pradesh, India *E-mail: vipin.a@invertis.org Abstract Rabeprazole sodium (RSM) is a proton pump inhibitor used against peptic ulcer disease to ... Read More »

METHOD DEVELOPMENT AND VALIDATION OF EFAVIRENZ IN BULK AND PHARMACEUTICAL TABLET DOSAGE FORM BY USING UV–VISIBLE SPECTROPHOMETRIC METHOD

ABOUT AUTHOR Somsubhra Ghosh*, B. Rajni,  S. Vidyadhar, Dr. David Banji Department of Pharmaceutical Analysis and Quality Assurance, Nalanda College of pharmacy, Cherlapally, Nalgonda, Andhra Pradesh, India. E-mail : som_subhra_ghosh@yahoo.co.in ABSTRACT The present research work discusses the development of UV Spectrophotometric method for the determination of Efavirenz  in bulk and pharmaceutical capsule dosage form. The present method is simple, rapid, ... Read More »

Method development and validation for the simultaneous estimation of Nebivolol hydrochloride and S (-) Amlodipine besilate in tablet dosage form by RP – HPLC

About author Prabhakaran. V.*, Sekar. S., Baskar.E., Raghuprasath. V.R. Formulation Research and Development Department, The Madras Pharmaceuticals, Karapakkam, Chennai, Tamil Nadu, India. Email: rnd@madraspharma.com ABSTRACT High Performance Liquid Chromatography method was developed and validated in a simple, specific and precise manner for Nebivolol HCl and Amlodipine besilate in a combined solid dosage form. Nebivolol hydrochloride, a long acting, cardioselective β ... Read More »

METHOD DEVELOPMENT AND ITS VALIDATION FOR QUANTITATIVE SIMULTANEOUS DETERMINATION OF DEXAMETHASONE AND GATIFLOXACIN IN OPHTHALMIC SOLUTION BY RP-HPLC

About author : Ankit Agarwal*, Subhash Dadhich, Sunil Kumar Tiwari, Kashyap Nagariya R & D Division, Ahlcon Parenterals (I) Ltd., Bhiwadi, Rajasthan, India *e-mail: ankitagarwal005@gmail.com ABSTRACT : To develop a simple, rapid and accurate HPLC method for simultaneous quantitative determination of Dexamethasone and Gatifloxacin in ophthalmic solution. Chromatographic separation was achieved with PDA detector using Inertsil C18, 250 x 4.6mm, ... Read More »

Method Validation in Pharmaceutical Analysis

Method Validation in Pharmaceutical Analysis J. Ermer and J. H. McB. Miller Methods used in pharmaceutical analysis must be sufficiently accurate, specific, sensitive and precise to conform to the regulatory requirements as set out in the relevant guidelines of “The International Conference of Technical Requirements for the Registration of Pharmaceutical for Human Use ” (ICH), which are applied by the ... Read More »

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